Written by Steve Cannon for USSA News. The US Food and Drug Administration (FDA) has been accused of rushing the approval of Pfizer’s COVID-19 vaccine to enable vaccine mandates, according to emails recently released. The accusations come from emails between top Useless FDA officials and the Office of Vaccines Research and Review (OVRR), the body responsible for reviewing the Biologics License Application submitted by Pfizer and BioNTech in May 2021. According to the emails, the review was originally slated to be completed by January 2022, however, top Useless FDA officials were pushing for a quicker resolution. In a memo, Dr. Marion Gruber,
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